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127671

Sigma-Aldrich

3-Aminobenzoic acid

98%, for peptide synthesis

Synonym(s):

3-Aminobenzenecarboxylic acid, 3-Carboxyaniline, m-Aminobenzoic acid, Aniline-3-carboxylic acid

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About This Item

Linear Formula:
H2NC6H4CO2H
CAS Number:
99-05-8
Molecular Weight:
137.14
Beilstein/REAXYS Number:
471603
EC Number:
202-724-4
MDL number:
MFCD00007795
UNSPSC Code:
12352106
PubChem Substance ID:
24847793
NACRES:
NA.22

product name

3-Aminobenzoic acid, 98%

assay

98%

reaction suitability

reaction type: solution phase peptide synthesis

mp

178-180 °C (lit.)

application(s)

peptide synthesis

SMILES string

Nc1cccc(c1)C(O)=O

InChI

1S/C7H7NO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,8H2,(H,9,10)

InChI key

XFDUHJPVQKIXHO-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

302.0 °F - closed cup

flash_point_c

150 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Lari Lehtiö et al.
Journal of medicinal chemistry, 52(9), 3108-3111 (2009-04-10)
Poly(ADP-ribose) polymerases (PARPs) activate DNA repair mechanisms upon stress- and cytotoxin-induced DNA damage, and inhibition of PARP activity is a lead in cancer drug therapy. We present a structural and functional analysis of the PARP domain of human PARP-3 in
M Wakselman et al.
Journal of medicinal chemistry, 36(11), 1539-1547 (1993-05-28)
In order to obtain selective suicide substrates of trypsin-like proteases including plasminogen activators, plasmin, and thrombin, a series of cyclopeptides cyclo[Arg or Lys-aB(CH2X)-Gly4], in which a substituted o- or m-aminobenzoyl group constitutes a latent electrophile, have been prepared. Treatment of
J T Wachsman
Mutation research, 350(1), 25-34 (1996-02-19)
There is compelling evidence for the central role of oxidative damage in the aging process and for the participation of reactive oxygen species in tumor initiation and promotion. Caloric restriction (CR) or energy restriction retards age-associated increases in mitochondrial free-radical
Marija Gizdavic-Nikolaidis et al.
Macromolecular bioscience, 10(12), 1424-1431 (2010-09-16)
Nanofibrous blends of HCl-doped poly(aniline-co-3-aminobenzoic acid) (3ABAPANI) copolymer and poly(lactic acid) (PLA) were fabricated by electrospinning solutions of the polymers, in varying relative proportions, in dimethyl sulfoxide/tetrahydrofuran mixture. The morphology, mechanical and electrical properties of the nanofibers were characterized and
A J Watson et al.
Gastroenterology, 109(2), 472-482 (1995-08-01)
H2O2 causes DNA damage, which activates poly(adenosine diphosphate ribose) polymerase (PARP), a nuclear enzyme that uses nicotinamide adenine dinucleotide (NAD) as a substrate. When DNA strand breaks are extensive, consumption of NAD by PARP can cause adenosine triphosphate depletion. The
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